Allele Registry

Canonical Allele Identifier: PA095165

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV000018589

RCV001507917

RCV001844014

RCV002496404

ClinVar Variation:

17060

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Arg592Gln	CA257691 NM_000064.4:c.1775G>A